Chattonella

The Chattonella species contain an ectoplasm with vacuoles, chloroplasts, and mucocysts and an endoplasm with a nucleus and other organelles. C. minima has an identical morphological structure to C. antiqua, so researchers are developing ways to search for the gene responsible for differentiating between the different Chattonella strains. The only currently known difference between the two strains is the number of chromosomes; C. minima contains 90-110 chromosomes while C. marina contains 29 chromosomes. Chattonella algal blooms synthesis is compared to "diatom resting hypothesis" with the only major difference being that Chattonella cysts can germinate in the dark as opposed to diatoms which can germinate only in sunlight. Factors such as water temperature, salinity, irradiance, and nutrients each contribute to the growth of Chattonella. == Environmental impact ==

Algal species can be beneficial, neutral, or harmful to environmental ecosystems. Three of these species, C. antiqua, C. marina, and C. ovata, contribute the growing problem of harmful algal blooms (HAB). Chattonella outbreaks are known to be enhanced by eutrophication. C. verruculosa was originally categorized with these toxic species, but further phylogenetic analysis showed it actually belonged to class Dictyochophyceae, not Raphidophyceae. These harmful algal species trigger the necrosis of gill cells in fish. More specifically, the toxins produce reactive oxygen species that disrupt oxygen transport and ultimately lead to suffocation. Fish species such as Thunnus maccoyii, Seriola quinqueradiata, and others are declining rapidly in Australia, Japan, India, China, Brazil, Mexico, and USA, greatly affecting fishing industries. As HABs become more common, more research is dedicated to preventing these outbreaks. == Analysis methods ==

To prevent Chattonella HABs, the individual species must first be studied. A technique using monoclonal antibodies can be used to identify the genus, while the RAPD reaction can be used to distinguish between different species within the genus. Other researchers use PCR-RFLP is also used to identify species of Chattonella. They sequence ITS rDNA and rRNA, and mitochondrial DNA of the species to try to target the highly variable regions with molecular markers. Inverted optical microscopes and scanning electron microscopes (SEM) are also used to compare cell size and structure of different Chattonella species. == References ==